Below is a partially filled in complementation table. Please answer the following questions. 1 2 3 4 5 6 1 2 I 3 4 5 6 + + I a. If you were to perform a complementation test with mutants 1 and 2, what would be the result? [ Select] b. If you were to perform a complementation test with mutants 5 and 6, what would be the result? [Select] c. If you were to perform a complementation test with mutants 3 and 4, what would be the result? [Select]
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- What is a complementation test?A RFLP is discovered that is linked to the gene for Duchenne’s muscular dystrophy (DMD). DMD is an X-linked, recessive trait. The RFLP is 2 map units from the gene for DMD. Consider the following pedigree and Southern blot using a probe that hybridizes to the RFLP. Which band/s is/are associated with DMD? What is the genotype for individuals 3 and 4? (Remember, this is an X linked disease, so use X’s and Y’s to denote). Individual 9 married a man who does NOT have muscular dystrophy, and she is pregnant. DMD is an X-linked trait. What is the probability for their child to have DMD? An amniocentesis is performed and it is determined that 9’s child in utero has only a 10 kb band that hybridizes to the same probe used above. What can you say about the child now?What will be the results of the following crosses, where N is black, n is brown, L is short hair and l is long hair. Make the tables and the corresponding explanation: 1. Crossing a Nnll woman dog with a Nnll dog. 2. Crossing a NnLl woman dog with a NnLl dog 3. Crossing a woman dog nnLl with a dog NNll
- Why do the geneticists use the complementation experiment? Explain complementation with an example that shows the application of this process.Can one gene be in two different complementation groups? More specifically, based on the data in this picture, is gene number 5 in two complementation groups with genes 1 and 8? making a total of 5 different complementation groups.Please label the tetrad type in the table as PD (parental ditype), NPD (non parental ditype) or T (tetratype) and answer the following questions a) Are the genes linked? Please explain SPECIFICALLY how you can distinguish between linked and unlinked genes in this instance. b) If the two genes are linked, calculate the % recombination between ser and thr. Show the formula used, as well as all of your calculations. c) Draw a single map illustrating the arrangement of the two genes on the chromosome with respect to each other and to the centromere of the chromosome. Make sure to map ALL three distances
- In an analysis of five rII mutants, complementation testing yielded the following results:Homozygous wild-type male mice (AA BB CC) were crossed with triplemutant female mice (aa bb cc), forming an F1 generation with the followinggenotype (Aa Bb Cc). The F1 males were crossed with triple mutantfemales, forming the following F2 phenotypes”“a B c” 3“A b C” 3“a b c” 8“A B c” 5“a b C” 5“A B C” 8“a B C” 6“A b c” 6 44 Determine the sequence of the genesHOW DO I SOLVE THIS STEP BY STEP: Recent studies suggest that having the A blood type increases the risk of serious complications for patients suffering from COVID-19. Sarah doesn't know her blood type, but she knows her father is type O and her mother is type AB. What is the probability, from 0 to 100 percent, that Sarah is blood type A? Enter a single whole number from 0 to 100. If you think the answer is a fraction, then round to the nearest whole number.
- What is Complementation Analysis ?Could someone please help me with this grade 11 bio dihybrid cross problem in detail and how to solve this question, using a strategy? Assume that curly hair (C) is dominant to straight hair. Albinism (P ) is recessive to normal skin pigmentation. A woman who is heterozygous for curly hair and albinism has a child. The father is homozygous dominant for curly hair and has albinism. (a) Determine the possible phenotypes for their child. (double-crossing, Puneet square)(b) Calculate the four different probabilities of a child beingboth a male and of each phenotype.(c) What is the probability that the child will expressalbinism and have curly hair like his father?A. Look at the pedigree, and DISREGARD individual II-8 for the moment. Is the pattern of inheritance of Unetan syndrome dominant or recessive? You may assume that the gene is FULLY-PENETRANT in this family. Please give two specific reasons that support your conclusion. B. Now, looking at BOTH the pedigree AND at the Southern blot, is this trait autosomal, X-linked, or Y-linked? Please give two specific reasons that support your conclusion. Once again, disregard II-8 for the moment. One of your two reasons must refer specifically to evidence present in the Southern blot. C. Define the gene alleles associated with Unetan syndrome. Your alleles MUST be consistent with the pattern of inheritance, AND your genetic notation must be consistent with that used throughout the course. Unetan syndrome allele: ________ Normal allele: ________